“…Another absorption peak is also observed at 2005 cm À1 , which can be attributed due to carbonate ion impurities. 17 Figure 1(c) shows the FTIR spectra of PANI-PbTiO 3 composites for 50 wt% of PbTiO 3 in PANI where the important peaks are observed; peak at 587 cm À1 corresponds to Ti-O vibration, peak at 802 cm À1 is due to C-H vibration of para coupled benzene ring, peak at 1142 cm À1 is due to C-O stretching, peak at 1302 cm À1 is due to C-O-C stretching (C-N stretching), peak at 1478 cm À1 is due to CH 2 bending, peak at 1560 cm À1 is due to C 5 C quinoid ring, and peak at 2923 cm À1 is due to C-H stretching, indicating the presence of PbTiO 3 in PANI. On comparing the major intense peaks observed in FTIR spectra of pure PANI, pure PbTiO 3 , and PANI-PbTiO 3 composites, it is noticed that intensity peaks observed in PANI-PbTiO 3 composites do not show much resemblance to that of the either PANI or PbTiO 3 .…”